Patterns and Outcomes of Neurosurgery in England Over a Five-year Period

October 14, 2021 updated by: Ryan Mathew, University of Leeds

Patterns and Outcomes of Neurosurgery in England Over a Five-year Period: a National Retrospective Cohort Study

Neurosurgical practice has seen many important changes over several decades with advances in treatments and the types of patients treated. Neurosurgical procedures have evolved, and as outcomes have improved the number of patients being treated has increased.

There are no recent evaluations of national neurosurgical practice in the United Kingdom (UK), with the last prospective cohort studies being Safe Neurosurgery 1993 and Safe Neurosurgery 2000. More recent studies of neurosurgical services have been based on data from single institutions or surgeons and these may not give a representative picture of practice nationally.

Recent national quality improvement programmes for neurosurgery in England (such as the National Neurosurgical Audit Programme (NNAP) and Cranial Neurosurgery and Spinal Surgery Getting It Right First Time (GIRFT) Programmes) have focused on using national hospital administrative datasets. To be effective, quality improvement initiatives require robust outcome measures and quality (process) indicators. Currently, there is a lack of validated quality indicators for neurosurgery, with practice often being described using generic measures such as readmission and reoperation rates and length of stay. Many studies have been able to derive these common outcome measures, but it may also be possible to produce indicators specific to neurosurgery.

The aim of this observational study was firstly to describe the current pattern of neurosurgical admissions and procedures in England, and thereby given an overview of the epidemiology of neurosurgical patients. Secondly, it aims to investigate the range of outcome measures that might be produced from hospital administrative data and use these to assess the quality of care in neurosurgery.

Study Overview

Study Type

Observational

Enrollment (Actual)

371418

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

All admissions to neurosurgical units in the National Health Service (NHS) in England. This covers any patients in England who required neurosurgical care, except those admitted to Private Providers of neurosurgical care.

Description

Inclusion Criteria:

  • All admissions to neurosurgical units in the National Health Service (NHS) in England.

Exclusion Criteria:

  • Records with poor quality data (e.g. no data for clinical diagnoses).
  • Patients under 18 years that were admitted to an adult neurosurgical unit.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Elective neurosurgery
Any elective neurosurgical procedure.
Any neurosurgical procedure in the National Neurosurgical Audit Programme (NNAP) Coding Framework of neurosurgical procedures.
Non-elective neurosurgery
Any non-elective neurosurgical procedure.
Any neurosurgical procedure in the National Neurosurgical Audit Programme (NNAP) Coding Framework of neurosurgical procedures.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Length of stay
Time Frame: From date of admission to date of discharge from hospital; assessed up to 60 months.
Length of the hospital admission to neurosurgery
From date of admission to date of discharge from hospital; assessed up to 60 months.
Additional inpatient neurosurgical procedure rate
Time Frame: From date of admission to date of discharge from hospital; assessed up to 60 months.
A further neurosurgical procedure in admissions where patients have had a primary (main) neurosurgical procedure.
From date of admission to date of discharge from hospital; assessed up to 60 months.
Proportion of patients discharged home
Time Frame: Determined on date of discharge from hospital; assessed up to 60 months.
Proportion of patients discharged to their normal address.
Determined on date of discharge from hospital; assessed up to 60 months.
In-patient mortality rate
Time Frame: From date of the neurosurgical procedure through date of death from any cause (in-patient deaths only); assessed up to 60 months.
In-patient mortality after a neurosurgical procedure.
From date of the neurosurgical procedure through date of death from any cause (in-patient deaths only); assessed up to 60 months.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: Ryan Mathew, University of Leeds

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

April 1, 2013

Primary Completion (ACTUAL)

March 31, 2018

Study Completion (ACTUAL)

March 31, 2018

Study Registration Dates

First Submitted

September 14, 2021

First Submitted That Met QC Criteria

October 14, 2021

First Posted (ACTUAL)

October 27, 2021

Study Record Updates

Last Update Posted (ACTUAL)

October 27, 2021

Last Update Submitted That Met QC Criteria

October 14, 2021

Last Verified

October 1, 2021

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • NNAP002

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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